HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31859754A>T , CM000668.2:g.31859754A>T | GRCh38 |
NC_000006.11:g.31827531A>T , CM000668.1:g.31827531A>T | GRCh37 |
NC_000006.10:g.31935510A>T | NCBI36 |
NG_008201.1:g.8179T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.1213T>A MANE Select | ENSP00000364782.4:p.Ser405Thr | |
ENST00000677054.1:n.2552T>A | ||
ENST00000677512.1:n.1490T>A | ||
ENST00000678869.1:n.1801T>A | ||
ENST00000375631.4:c.1213T>A | ENSP00000364782.4:p.Ser405Thr | |
ENST00000480384.1:n.1512T>A | ||
ENST00000491768.5:c.*323T>A | ENSP00000433127.1:n.*323T>A | |
ENST00000495807.1:n.2521T>A | ||
NM_000434.3:c.1213T>A | NP_000425.1:p.Ser405Thr | |
NM_000434.4:c.1213T>A MANE Select | NP_000425.1:p.Ser405Thr |